Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Muckelab

Rahway, New Jersey, USA
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid (3 days onsite, 1 day remote)
Gmp manufacturing facilities experience
Drug product processing knowledge
Leading quality investigations
Muckelab is seeking a Specialist in Process Engineering for their Oral Solid Dosage team in Rahway, New Jersey. The role involves leading clinical manufacturing, ensuring quality and safety in drug production, and requires experience in GMP environments

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products leveraging pharmaceutical unit operations.
  • This role will lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
  • The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

Muckelab is seeking a Specialist in Process Engineering for their Oral Solid Dosage team in Rahway, New Jersey. The role involves leading clinical manufacturing, ensuring quality and safety in drug production, and requires experience in GMP environments.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • GMP manufacturing facilities experience
  • Drug product processing knowledge
  • Leading quality investigations
  • Change management experience
  • Oral Solid Dosage manufacturing

Nice-to-have

  • Collaboration and innovation culture
  • Independent problem-solving willingness
  • Cross-functional relationship building
  • Scientific rigor in manufacturing

Key Requirements

  • Bachelor of Science with 2 years relevant experience
  • Master's degree with 1 year relevant experience
  • Experience in executing in GMP manufacturing
  • Experience in leading and supporting quality investigations

Work Rights

Not specified

Tailored Resume

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